Canonical Allele Identifier: CA3341932

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810758G>A , CM000667.2:g.90810758G>A	GRCh38
NC_000005.9:g.90106575G>A , CM000667.1:g.90106575G>A	GRCh37
NC_000005.8:g.90142331G>A	NCBI36
NG_007083.1:g.256959G>A
NG_007083.2:g.286415G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15498G>A MANE Select	NP_115495.3:p.Thr5166=
ENST00000405460.9:c.15498G>A MANE Select	ENSP00000384582.2:p.Thr5166=
NM_032119.3:c.15498G>A	NP_115495.3:p.Thr5166=
NR_003149.1:n.15511G>A
NR_003149.2:n.15514G>A
ENST00000405460.6:c.15498G>A	ENSP00000384582.2:p.Thr5166=
ENST00000425867.2:c.2481G>A	ENSP00000392618.2:p.Thr827=
ENST00000425867.3:c.4452G>A	ENSP00000392618.3:p.Thr1484=
ENST00000638510.1:n.2765G>A
ENST00000639431.1:c.265+134549G>A	ENSP00000491057.1:n.265+134549G>A
ENST00000640407.1:c.1908G>A	ENSP00000491425.1:p.Thr636=
XM_011543675.1:c.15495G>A	XP_011541977.1:p.Thr5165=
XM_011543676.1:c.15417G>A	XP_011541978.1:p.Thr5139=
XM_011543677.1:c.12801G>A	XP_011541979.1:p.Thr4267=
XM_017009963.2:c.15519G>A	XP_016865452.1:p.Thr5173=
XM_017009964.2:c.15516G>A	XP_016865453.1:p.Thr5172=
XM_017009965.1:c.15516G>A	XP_016865454.1:p.Thr5172=
XM_017009966.2:c.15438G>A	XP_016865455.1:p.Thr5146=
XM_017009967.1:c.15423G>A	XP_016865456.1:p.Thr5141=
XM_017009968.2:c.15339G>A	XP_016865457.1:p.Thr5113=
XM_017009969.2:c.15519G>A	XP_016865458.1:p.Thr5173=
XM_017009971.2:c.*452G>A	XP_016865460.1:n.*452G>A
XM_017009972.1:c.8637G>A	XP_016865461.1:p.Thr2879=
XM_017009973.1:c.8616G>A	XP_016865462.1:p.Thr2872=